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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Pyrazine, 1H-imidazol-2-yl-

c1cnc(cn1)c1ncc[nH]1 Request for Quotation
Chemical Name: Pyrazine, 1H-imidazol-2-yl-
CAS Number: 119165-68-3
Product Number: AG000I9S(AGN-PC-02SP8X)
Synonyms:
MDL No:
Molecular Formula: C7H6N4
Molecular Weight: 146.1493

Identification/Properties

Computed Properties
Molecular Weight:
146.153g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
146.059g/mol
Monoisotopic Mass:
146.059g/mol
Topological Polar Surface Area:
54.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
128
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(1H-Imidazol-2-yl)pyrazine is a versatile compound widely utilized in chemical synthesis as a key building block for creating complex organic molecules. Due to its unique structure, this compound serves as a valuable intermediate in the development of pharmaceuticals, agrochemicals, and materials science. Its aromatic imidazole and pyrazine moieties confer reactivity and selectivity in various synthetic pathways, allowing for the creation of novel compounds with diverse functionalities. In organic synthesis, this compound can be employed in the formation of heterocyclic structures, which are essential in drug discovery and development. Its compatibility with a range of functional groups enables chemists to construct elaborate molecular frameworks efficiently. Furthermore, the presence of both nitrogen heterocycles enhances the potential for coordination chemistry, making it a desirable ligand in catalysis and metal-organic frameworks. The application of 2-(1H-Imidazol-2-yl)pyrazine in chemical synthesis showcases its significance as a valuable tool in the molecular design and fabrication of advanced materials with tailored properties.